HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1921893Generated: October 31, 2026
Ammonium Chloride → 4-[3-(3,5-Difluoro-4-triisopropylsilanyloxybenzyl)-4-hydroxybutyl]benzonitrile
https://huagongshe.com/reaction/1921893
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 4-(4-Cyanophenyl)-2-(3,5-difluoro-4-triisopropylsilanyloxybenzyl)butanoic acid | HCID 57971899 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-[3-(3,5-Difluoro-4-triisopropylsilanyloxybenzyl)-4-hydroxybutyl]benzonitrile | HCID 57971916 | — |
Reaction Steps
4879 mg (10 mmol) of 4-(4-cyanophenyl)-2-(3,5-difluoro-4-triisopropylsilanyloxybenzyl)butanoic acid are dissolved in 244 ml of THF and cooled to −10° C. under argon. Then 20.01 ml (20.01 mmol) of a 1 M borane-THF complex solution are added dropwise, and the mixture is stirred at 0° C. until reaction is complete. The mixture is hydrolyzed with saturated ammonium chloride solution and extracted with diethyl ether, and the combined organic phases are concentrated. The resulting crude product is purified by chromatography on silica gel (mobile phase: cyclohexane/ethyl acetate 9:1→4:1→2:1→1:1). 2705 mg (57% of theory) of the title compound are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08173704B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-dd3d14d88675464fb1d8f2c7515dbea2 |
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| Source note | uspto-grants-2012_05 |
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